Canonical Allele Identifier: CA176658608

Gene: CLXN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.48729838C>A , CM000670.2:g.48729838C>A	GRCh38
NC_000008.10:g.49642397C>A , CM000670.1:g.49642397C>A	GRCh37
NC_000008.9:g.49804950C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024593.4:c.353G>T MANE Select	NP_078869.1:p.Gly118Val
ENST00000262103.8:c.353G>T MANE Select	ENSP00000262103.3:p.Gly118Val
NM_001142857.1:c.197G>T	NP_001136329.1:p.Gly66Val
NM_001142857.2:c.197G>T	NP_001136329.1:p.Gly66Val
NM_001363973.1:c.197G>T	NP_001350902.1:p.Gly66Val
NM_001363973.2:c.197G>T	NP_001350902.1:p.Gly66Val
NM_001363973.3:c.197G>T	NP_001350902.1:p.Gly66Val
NM_001363974.1:c.197G>T	NP_001350903.1:p.Gly66Val
NM_001363974.2:c.197G>T	NP_001350903.1:p.Gly66Val
NM_024593.3:c.353G>T	NP_078869.1:p.Gly118Val
NR_024605.1:n.324-14G>T
NR_024605.2:n.281-14G>T
NR_024605.3:n.281-14G>T
NR_157026.1:n.324-14G>T
NR_157027.1:n.326-726G>T
NR_157027.2:n.326-726G>T
ENST00000262103.7:c.353G>T	ENSP00000262103.3:p.Gly118Val
ENST00000433756.1:c.197G>T	ENSP00000400873.1:p.Gly66Val
ENST00000519425.1:n.288G>T
ENST00000521002.5:n.292-726G>T
ENST00000521701.5:c.164-14G>T	ENSP00000430374.1:n.164-14G>T
ENST00000521721.1:n.507G>T
ENST00000522254.5:c.105G>T
ENST00000523092.5:c.197G>T	ENSP00000430765.1:p.Gly66Val
XM_005251303.1:c.353G>T	XP_005251360.1:p.Gly118Val
XM_005251304.2:c.197G>T	XP_005251361.1:p.Gly66Val
XM_011517589.1:c.353G>T	XP_011515891.1:p.Gly118Val
XM_011517590.1:c.167G>T	XP_011515892.1:p.Gly56Val
XM_011517591.1:c.167G>T	XP_011515893.1:p.Gly56Val
XM_011517591.2:c.167G>T	XP_011515893.1:p.Gly56Val
XM_017013827.1:c.167G>T	XP_016869316.1:p.Gly56Val
XM_017013828.1:c.320-14G>T	XP_016869317.1:n.320-14G>T
XM_024447270.1:c.353G>T	XP_024303038.1:p.Gly118Val
XM_024447271.1:c.353G>T	XP_024303039.1:p.Gly118Val
XM_024447272.1:c.353G>T	XP_024303040.1:p.Gly118Val
XM_024447273.1:c.167G>T	XP_024303041.1:p.Gly56Val
XM_024447274.1:c.167G>T	XP_024303042.1:p.Gly56Val
XR_002956645.1:n.470G>T